Long time coming
I was diagnosed in 1992 and it was benign mostly until 2013. I'm now SPMS and as an ex rugby player I just say 'bring it on, do your worst'. I won't give up! I'm new here so still lots to read lol
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X-rugby player from W-ton had MS for 30+ years now still fighting it every day!!
We will be fighting..every day until we pass. Not everyone has the same symptoms. That's why there will be no cure. I told my neurologist this. Which he already knew. I said, there will be no cure. He Said, the same thing. I've been fighting for 30 years. I take one day at a time. Like everyone else. That's all we can do. I also feel that, There is someone else who's worse of than me. Love ❤️ everyone I'm new here.